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Mostrati risultati da 367 a 386 di 587
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1999 mtDNA history of the Cayapa Amerinds of Ecuador: Detection of additional founding lineages for the native American populations Rickards, O; MARTINEZ-LABARGA, Mc; Lum, J; De Stefano, G; Cann, R Articolo su rivista
13-ago-2020 mTOR inhibition leads to SRC-mediated EGFR internalisation and degradation in glioma cells Colella, B; Colardo, M; Iannone, G; Contadini, C; Saiz-Ladera, C; Fuoco, C; Barila', D; Velasco, G; Segatto, M; Di Bartolomeo, S Articolo su rivista
1-gen-2008 Multiple advantageous amino acid variants in the NAT2 gene in human populations Luca, F; Bubba, G; Basile, M; Brdicka, R; Michalodimitrakis, E; Rickards, O; Vershubsky, G; Quintana, M; L, K; Ai, ; Novelletto, A Articolo su rivista
1-gen-2013 Multiple and differentiated contributions to the male gene pool of pastoral and farmer populations of the African Sahel Buckova, J; Cerny, V; Novelletto, A Articolo su rivista
14-ott-2010 Multiple modification and protein interaction signals drive the Ring finger protein 11 (RNF11) E3 ligase to the endosomal compartment Santonico, E; Belleudi, F; Panni, S; Torrisi, M; Cesareni, G; Castagnoli, L Articolo su rivista
1-gen-2020 A multivariate statistical approach for the estimation of the ethnic origin of unknown genetic profiles in forensic genetics Alladio, E; Della Rocca, C; Barni, F; Dugoujon, J-; Garofano, P; Semino, O; Berti, A; Novelletto, A; Vincenti, M; Cruciani, F Articolo su rivista
1-gen-2010 Musei e laboratori: un lavoro comune per la salvaguardia delle tartarughe marine Garofalo, L; Carlini, R; Novelletto, A Altro
1-gen-2003 Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency Akaboshi, S; Hogema, B; Novelletto, A; Malaspina, P; Salomons, G; Maropoulos, G; Jakobs, C; Grompe, M; Gibson, K Articolo su rivista
1-gen-2019 Myo-REG: A portal for signaling interactions in muscle regeneration Palma, A; Perpetuini, Ac; Ferrentino, F; Fuoco, C; Gargioli, C; Giuliani, G; Iannuccelli, M; Licata, L; Micarelli, E; Paoluzi, S; Perfetto, L; Petrilli, Ll; Reggio, A; Rosina, M; Sacco, F; Vumbaca, S; Zuccotti, A; Castagnoli, L; Cesareni, G Articolo su rivista
1-gen-1998 Network analyses of Y-chromosomal types in Europe, Northern Africa, and Western Asia reveal specific patterns of geographic distribution Malaspina, P; Cruciani, F; Ciminelli, Bm; Terrenato, L; Santolamazza, P; Alonso, A; Banyko, J; Brdicka, R; Garcia, O; Gaudiano, C; Guanti, G; Kidd, K; Lavinha, J; Avila, M; Mandich, P; Moral, P; Qamar, R; Mehdi, S; Ragusa, A; Stefanescu, G; Caraghin, M; Tyler Smith, C; Scozzari, R; Novelletto, A Articolo su rivista
1-gen-2003 New data on the world distribution of paraoxonase (PON1 Gln 192 -> Arg) gene frequencies Scacchi, R; Corbo, R; Rickards, O; De Stefano, G Articolo su rivista
1-gen-2014 New insights into the distribution of apoe polymorphism in the iberian peninsula. The case of Andalusia (Spain) Reales, G; Hernandez, Cl; Dugoujon, J-; Novelletto, A; Cuesta, P; Fortes-Lima, C; Rodriguez, Jn; Calderon, R Articolo su rivista
1-gen-2021 New insights into the evolution of human y chromosome palindromes through mutation and gene conversion Bonito, M; D'Atanasio, E; Ravasini, F; Cariati, S; Finocchio, A; Novelletto, A; Trombetta, B; Cruciani, F Articolo su rivista
1-gen-2004 A new model for prediction of the age of onset and penetrance for Huntington’s disease based on CAG length. Langbehn, D; Brinkman, R; Falush, D; Paulsen, J; Hayden, M; Huntington’s Disease Collaborative, G; Novelletto, A Articolo su rivista
15-gen-2009 Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic Ataxia Veneziano, L; Guida, S; Mantuano, E; Bernard, P; Tarantino, P; Boccone, L; Hisama, F; Carrera, P; Iodice, C; Frontali, M Articolo su rivista
1-gen-2006 Non disjunction rates of mouse chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes. II. The effects of trivalent combinations and genetic background Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M Articolo su rivista
1-gen-2004 Nondisjunction rates of mouse specific chromosomes involved in heterozygous Rb rearrangements measured by chromosome painting of spermatocytes II. I. The effects of the number of trivalents Scascitelli, M; Gustavino, B; Pacchierotti, F; Spirito, F; Rizzoni, M Articolo su rivista
1-gen-2013 A novel approach to represent and compare RNA secondary structure - Tesi di dottorato
1-gen-2019 Novel mutations in two unrelated Italian patients with SSADH deficiency Balzarini, M; Rovelli, V; Paci, S; Rigoldi, M; Sanna, G; Pillai, S; Asunis, M; Parini, R; Ciminelli, Bm; Malaspina, P Articolo su rivista
1-gen-2008 A novel sampling design to explore gene-longevity associations: the ECHA study. De Rango, F; Dato, S; Bellizzi, D; Rose, G; Marzi, E; Cavallone, L; Franceschi, C; Skytthe, A; Jeune, B; Cournil, A; Robine, J; Gampe, J; Vaupel, J; Mari, V; Feraco, E; Passarino, G; Novelletto, A; De Benedictis, G Articolo su rivista
Mostrati risultati da 367 a 386 di 587
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